Maternal acellular pertussis vaccination in mice impairs cellular immunity to Bordetella pertussis infection in offspring.

Maternal acellular pertussis vaccination in mice impairs cellular immunity to Bordetella pertussis infection in offspring.
复制标题

DOI:
10.1172/jci.insight.167210
复制
发表时间:
2023-09-22
期刊:
影响因子:
8
通讯作者:
Locht, Camille
Locht, Camille
中科院分区:
医学1区
文献类型:
--
作者:
Dubois, Violaine;Chatagnon, Jonathan;Depessemier, Manon;Locht, Camille

文献摘要

参考文献

相似文献

鉴于百日咳死灰复燃,一些国家在怀孕期间引入了产妇破伤风、白喉和无细胞百日咳(aP)疫苗接种,以保护年幼婴儿免受严重百日咳的侵害。虽然对疾病有保护作用,但母体接种aP疫苗对后代细菌定植的影响尚不清楚。在这里,我们使用小鼠模型来证明母体在怀孕前或怀孕期间接种aP免疫可以保护幼崽免受百日咳博德特拉的肺部定植。然而,母体接种aP疫苗通过抑制产生il -17的常驻记忆T细胞的自然募集和随后的中性粒细胞流入鼻腔组织,特别是那些具有促炎和细胞毒性的中性粒细胞,导致百日咳鼻携带时间明显延长。接种aP后鼻腔携带时间延长是由于IL-4信号传导,因为IL-4Rα - / -小鼠鼻腔携带时间延长被消除。母亲接种aP疫苗的效果可经胎盘转移给后代或通过母乳喂养,并持续到成年。因此,母亲接种aP疫苗可能会增加百日咳储存库。
Given the resurgence of pertussis, several countries have introduced maternal tetanus, diphtheria, and acellular pertussis (aP) vaccination during pregnancy to protect young infants against severe pertussis. Although protective against the disease, the effect of maternal aP vaccination on bacterial colonization of the offspring is unknown. Here, we used a mouse model to demonstrate that maternal aP immunization, either before or during pregnancy, protects pups from lung colonization by Bordetella pertussis. However, maternal aP vaccination resulted in significantly prolonged nasal carriage of B. pertussis by inhibiting the natural recruitment of IL-17–producing resident memory T cells and ensuing neutrophil influx in the nasal tissue, especially of those with proinflammatory and cytotoxic properties. Prolonged nasal carriage after aP vaccination is due to IL-4 signaling, as prolonged nasal carriage is abolished in IL-4Rα–/– mice. The effect of maternal aP vaccination can be transferred transplacentally to the offspring or via breastfeeding and is long-lasting, as it persists into adulthood. Maternal aP vaccination may, thus, augment the B. pertussis reservoir.
DOI: 10.4049/immunohorizons.2000076
发表时间: 2020-09-18
期刊: ImmunoHorizons
影响因子: --
作者:
Poudel B;Yorek MS;Mazgaeen L;Brown SA;Kanneganti TD;Gurung P
通讯作者: Gurung P
DOI: 10.4049/jimmunol.1004043
发表时间: 2011-06-15
期刊: Journal of immunology (Baltimore, Md. : 1950)
影响因子: --
作者:
Guan H;Nagarkatti PS;Nagarkatti M
通讯作者: Nagarkatti M
DOI: 10.1182/blood.v96.12.3866.h8003866_3866_3871
发表时间: 2000-12-01
期刊: BLOOD
影响因子: 20.3
作者:
Clerici, M;Saresella, M;Vigano, A
通讯作者: Vigano, A
DOI: 10.1016/j.cell.2016.04.055
发表时间: 2016-05-05
期刊: Cell
影响因子: 64.5
作者:
Koch MA;Reiner GL;Lugo KA;Kreuk LS;Stanbery AG;Ansaldo E;Seher TD;Ludington WB;Barton GM
通讯作者: Barton GM
T细胞重新进入成人胸腺,仅限于活化的T细胞。
DOI: 10.1084/jem.173.5.1039
发表时间: 1991-05-01
期刊: The Journal of experimental medicine
影响因子: --
作者:
Agus DB;Surh CD;Sprent J
通讯作者: Sprent J